Who Should Attend

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This workshop is designed for NHS/ Academic staff whose role involves monitoring clinical research governed by the regulations required for clinical trials of medicinal products. For example, monitors, research nurses, trial managers, project managers, pharmacy staff, R&D staff. Management staff involved with supervising monitors or managing oversight of research activity will also find this course of interest.

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Description

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It will be an interactive day with a combination of presentations, discussions and workshop. By the end of this workshop, participants will be able to:

• Define the purpose of monitoring clinical trials.

• Understand the role of pharmacy & labs in clinical trials.

• Plan and conduct Investigational Medicinal product (IMP) monitoring in Pharmacy.

• Ensure IMP are managed and dispensed to patients in accordance with the protocol.

• Monitor the system of controls governing the collection, processing, and storage of samples to ensure sample integrity and accurate results.

• Manage non-compliance(s)

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As it is only 1 day pre reading is required prior to attendance.